Canonical Allele Identifier: CA2054318687

Gene: LUM

Linked Data

• dbSNP Id: rs1880100153

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107333_91107334insGG , CM000674.2:g.91107333_91107334insGG	GRCh38
NC_000012.11:g.91501110_91501111insGG , CM000674.1:g.91501110_91501111insGG	GRCh37
NC_000012.10:g.90025241_90025242insGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+785_862+786insCC MANE Select	ENSP00000266718.4:n.862+785_862+786insCC
ENST00000266718.4:c.862+785_862+786insCC	ENSP00000266718.4:n.862+785_862+786insCC
ENST00000546642.1:n.612+785_612+786insCC
ENST00000548071.1:n.255+785_255+786insCC
NM_002345.3:c.862+785_862+786insCC	NP_002336.1:n.862+785_862+786insCC
NM_002345.4:c.862+785_862+786insCC MANE Select	NP_002336.1:n.862+785_862+786insCC